Treating the Symptoms of Vertigo in a Real-world Setting Using the OtoBand

Otolith Labs

Status: Completed

Conditions: Benign Paroxysmal Positional Vertigo; Vertigo; Vestibular Migraine; BPPV; Meniere Disease; Uncompensated Unilateral Vestibulopathy; Ménière's Vertigo; Labrynthitis; Migraine Associated Vertigo; Vestibular Disorder

Treatments: Device: Otoband Experimental; Device: Otoband Sham

Study type: Interventional

Funder types: Industry

Identifiers

NCT05960786

OLith10702

Details and patient eligibility

About

The goal of this virtual clinical trial is to determine the effectiveness of two study devices in providing temporary relief to adults aged 18-70 who suffer from symptoms of chronic vestibular vertigo.

The main question[s] it aims to answer are:

• Within an episode, is there a significant difference between the randomized study devices at the individual timepoints during the vertigo episode?
• Within an episode, is there evidence of quantitative treatment at each individual timepoint during the vertigo episode?

Participants will be:

• Enrolled up to 49 days; 14 days in Baseline Phase (no device) and 21 days in Treatment Phase (study device) for Study Arm 1 or 28 days in Treatment Phase (study device) for Study Arm 2
• Randomized and stratified into groups based on diagnosis to be assigned a study device
• Asked to use the study device as instructed by the study coordinator
• Asked to download a study app to submit daily diaries regarding their symptoms and use of device, and to participate in tele-health visits with study coordinators
• Asked to provide their vertigo diagnosis from their physician
• Compensated for their participation

Researchers will compare the randomized groups to see which groups respond better to which device.

Full description

This study is decentralized clinical trial. This study uses technology and and virtual meetings to communicate with study participants and collect study data. This study seeks to enroll until 36 participants in the Moderate or Worse (MoW) arm have completed the study, and until 72 participants have completed the Quality of Life (QoL) arm.

All study participants that meet all of the inclusion, none of the exclusion criteria, and sign informed consent will be enrolled in the study. Participants will complete a one day enrollment meeting and an approximately 14 day Baseline Phase.

After the Baseline Phase, participants will be placed in one of two groups Moderate or Worse (MoW) group or Quality of Life (QoL) group based on the data collected about their vertigo during the Baseline Phase.

Participants will then be randomized within their assigned group (MoW or QoL) at a 2:1 ratio to an active arm or sham arm to begin the Treatment Phase of the study. Participants will be sent a study device to use when they have a vertigo episode.

Participants that enroll in the study are expected to participate up to 49 days with virtual meetings at the approximate intervals:

MoW Group: Day 4, Day 16, Day 21, Day 24, Day 31, and Day 42 QoL Group : Day 4, Day 16, Day, 21, Day 24, Day 31, and Day 49

Participants will be required to complete the DHI (Dizziness Handicap Index), VSS (Vertigo Symptom Scale), Global Impression of Symptoms, and Global Impression of Change questionnaires.

Otolith Labs received Therapeutic Breakthrough Device designation by the FDA in May 2021.

Enrollment: 109 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• To be eligible to participate in this study, an individual must meet all the following criteria:

  • Diagnosed as having vestibular vertigo that is caused by one or more of:

    • Benign paroxysmal positional vertigo (BPPV)
    • Migraine associated vertigo (MAV, aka vertiginous migraines)
    • Meniere's disease (aka idiopathic endolymphatic hydrops)
    • Uncompensated unilateral vestibulopathy (such as arising from vestibular neuritis and labyrinthitis)

  • Vertigo that has been present for at least 90 days

  • Score greater than 35, and less than 91, on the Dizziness Handicap Inventory (corresponding to moderate to severe vertigo)

  • Smartphone, computer or tablet and access to internet for online enrollment, check-in and wrap-up meetings

  • Willingness to install and use the JotForm ePRO app

  • Residing in the United States

  • Willingness to be paid via Venmo or PayPal.

Exclusion criteria

• Surgery to the base of the skull within the last 6 months or plans for surgery to the skull during enrollment period
• Any skull or neck implants such as but not limited to a cochlear implant, vascular stents, bone conduction implant, or deep brain stimulation device
• History of vitreous detachment (aka floaters) in the last 90 days
• Superior canal dehiscence (aka third window) or otic capsule dehiscence
• Hyperacusis (aka hypersensitivity to loud sounds)
• Currently undergoing vestibular rehabilitation therapy or planning to start vestibular rehabilitation therapy during the study. (People who have completed vestibular rehabilitation therapy, but in whom vestibular vertigo persists, will be permitted to enroll)
• History of cerebrovascular disorders
• Posterior fossa tumors (brain tumors located in the caudal third of the skull)
• Vestibular schwannoma (non-cancerous tumor located on the vestibulo-cochlear nerve)
• Cerebellar degeneration (progressive worsening of neurons behind the brain stem)
• Taking benzodiazepines (e.g., clonazepam, lorazepam, diazepam) for vestibular issues.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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109 participants in 4 patient groups

1. Moderate or Worse (MoW) Arm

Experimental group

Description:

Participants will be randomized to use the Otoband as instructed by clinical coordinator per study protocol. There are 4 power levels, these participants will receive the experimental device.

Treatment:

Device: Otoband Experimental

2. Moderate or Worse (MoW) Arm

Sham Comparator group

Description:

Participants will be randomized to use the Otoband as instructed by clinical coordinator per study protocol. There are 4 power levels, these participants will receive the sham device.

Treatment:

Device: Otoband Sham

1. Quality of Life (QoL) Arm

Experimental group

Description:

Participants will be randomized to use the Otoband as instructed by clinical coordinator per study protocol. There are 4 power levels, these participants will receive the experimental device.

Treatment:

Device: Otoband Experimental

2. Quality of Life (QoL) Arm

Sham Comparator group

Description:

Participants will be randomized to use the Otoband as instructed by clinical coordinator per study protocol. There are 4 power levels, these participants will receive the sham device.

Treatment:

Device: Otoband Sham